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PACKS-4 (TM) ANALYZER

K912201 Class II Traditional
Decision Date
1991-08-16
Sponsor / Applicant
Helena Laboratories

Technical Specification

510(k) Submission ID K912201
Product Code JBY
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.6675
Decision Date 1991-08-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PACKS-4 (TM) ANALYZER received FDA 510(k) clearance under submission number K912201, sponsored by Helena Laboratories. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1991-08-16.

Classification & Regulation

This clearance is catalogued under FDA product code JBY and 21 CFR 864.6675, within the Hematology review panel as a Class II device.